5.33304

DSM1

≥97% (HPLC), solid, DHODH inhibitor, Calbiochem^®

• Synonym(e): DHODH Inhibitor, DSM1, 5-Methyl-N-(2-naphthyl)[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, Malaria Parasite Dihydroorotate Dehydrogenase Inhibitor, P. falciparum Dihydroorotate Dehydrogenase Inhibitor, Plasmodium falciparum Dihydroorotate Dehydrogenase Inhibitor; T
• Empirische Formel (Hill-System): C₁₆H₁₃N₅
• CAS-Nummer: 92872-51-0
• Molekulargewicht: 275.31
• MDL number: MFCD01099828
• UNSPSC Code: 12352200
• NACRES: NA.77
• PubChem Substance ID: 660996
• Assay: ≥97% (HPLC)
• Form: solid
• Quality level: 100
• Storage condition: OK to freeze, protect from light

Eigenschaften

• Produktname: DHODH Inhibitor, DSM1,
• assay: ≥97% (HPLC)
• Quality Level: 100
• form: solid
• potency: 15 nM K_i
• manufacturer/tradename: Calbiochem^®
• storage condition: OK to freeze, protect from light
• color: off-white
• solubility: DMSO: 50 mg/mL
• storage temp.: 2-8°C
• SMILES string: CC1=NC2=NC=NN2C(=C1)NC3=CC4=CC=CC=C4C=C3

Beschreibung

General description

A cell-permeable triazolopyrimidine compound that potently inhibits malaria parasite Plasmodium falciparum dihydroorotate dehydrogenase- (PfDHODH-) catalyzed electron transfer from FMNH₂ to Coenzyme Q₁₀ (CoQ or ubiquinone) in a potent (IC₅₀ = 47 nM), CoQ-competitive (K_i = 15 nM), and species-specific manner, without affecting PfDHODH-catalyzed electron transfer from DHO to FMN or the enzymatic activity of human DHODH (<5% inhibition at 100 µM). Reported to inhibit the proliferation of P. falciparum parasites (EC₅₀ = 79 nM against 3D7 strain) in vitro, including the drug-resistant strain Dd2 (EC₅₀ = 140 nM), while displaying no inhibitory potency against murine lymphocytic leukemia cell line L1210 even at concentrations as high as 10 µM. DSM1 is not recommended for in vivo use due to reduced plasma exposure upon repeat dosing in mice.

DHODH Inhibitor, DSM1, is a highly potent, competitive, tight-binding inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase (IC₅₀ = 47 nM; K_i = 15 nM).

Biochem/physiol Actions

Cell permeable: yes

Primary Target
Pf*DHODH

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

Guler, J.L., et al. 2013. PLoS Pathog.9, e1003375.

Ke, H., et al. 2011. Eukaryot. Cell.10, 1053.
Ganesan, S.M., et al. 2011. Mol. Biochem. Parasitol.177, 29.
Booker, M.L., et al. 2010. J. Biol. Chem.285, 33054.
Gujjar, R., et al. 2009. J. Med. Chem.52, 1864.
Phillips, M.A., et al. 2008. J. Med. Chem.51, 3649.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

Sicherheitshinweise

• Lagerklasse: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable